Evidence map›Paper›PMID 30703100›Full record

SynthesisPLoS medicine2019

Evidence of a causal relationship between body mass index and psoriasis: A mendelian randomization study.

Ashley Budu-Aggrey, Ben Brumpton, Jess Tyrrell, Sarah Watkins, Ellen H Modalsli, Carlos Celis-Morales, Lyn D Ferguson, Gunnhild Åberge Vie, Tom Palmer, Lars G Fritsche and 18 more

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in PLoS medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 124 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
124citing papers in PubMed, 6 pooled it
9.9field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

124 citing papers in PubMed, 6 syntheses or guidelines pooled it, 247 citations in OpenAlex.

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  17. A Bidirectional Mendelian Randomization Study of Androgenetic Alopecia and Obesity.Clinical, cosmetic and investigational dermatology · 2026
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64 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors at 7 institutions in 3 countries.

Ashley Budu-AggreyMedical Research Council (MRC) Integrative Epidemiology Unit, University of Bristol, Bristol, United Kingdom.ORCID 0000-0002-8911-2492
Ben BrumptonMedical Research Council (MRC) Integrative Epidemiology Unit, University of Bristol, Bristol, United Kingdom.
Jess TyrrellGenetics of Complex Traits, Institute of Biomedical and Clinical Science, University of Exeter Medical School, Royal Devon and Exeter Hospital, Exeter, United Kingdom.ORCID 0000-0002-9256-6065
Sarah WatkinsMedical Research Council (MRC) Integrative Epidemiology Unit, University of Bristol, Bristol, United Kingdom.ORCID 0000-0002-8034-8095
Ellen H ModalsliDepartment of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.ORCID 0000-0002-3061-1844
Carlos Celis-MoralesInstitute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0003-2612-3917
Lyn D FergusonInstitute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0002-6136-8349
Gunnhild Åberge VieDepartment of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.ORCID 0000-0003-1552-5291
Tom PalmerDepartment of Mathematics and Statistics, Lancaster University, Lancaster, United Kingdom.ORCID 0000-0003-4655-4511
Lars G FritscheK.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.ORCID 0000-0002-2110-1690
Mari LøsetK.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.
Jonas Bille NielsenDepartment of Internal Medicine, Division of Cardiology, University of Michigan Medical School, Ann Arbor, Michigan, United States of America.ORCID 0000-0002-6654-2852
Wei ZhouDepartment of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, Michigan, United States of America.ORCID 0000-0001-7719-0859
Lam C TsoiDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan, United States of America.ORCID 0000-0003-1627-5722
Andrew R WoodGenetics of Complex Traits, Institute of Biomedical and Clinical Science, University of Exeter Medical School, Royal Devon and Exeter Hospital, Exeter, United Kingdom.
Samuel E JonesGenetics of Complex Traits, Institute of Biomedical and Clinical Science, University of Exeter Medical School, Royal Devon and Exeter Hospital, Exeter, United Kingdom.ORCID 0000-0003-0153-922X
Robin BeaumontGenetics of Complex Traits, Institute of Biomedical and Clinical Science, University of Exeter Medical School, Royal Devon and Exeter Hospital, Exeter, United Kingdom.ORCID 0000-0003-0750-8248
Marit SaunesDepartment of Dermatology, St. Olav's Hospital, Trondheim University Hospital, Trondheim, Norway.
Pål Richard RomundstadDepartment of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.ORCID 0000-0003-2061-4336
Stefan SiebertInstitute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0002-1802-7311
Iain B McInnesInstitute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, United Kingdom.
James T ElderDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan, United States of America.ORCID 0000-0003-4215-3294
George Davey SmithMedical Research Council (MRC) Integrative Epidemiology Unit, University of Bristol, Bristol, United Kingdom.ORCID 0000-0002-1407-8314
Timothy M FraylingGenetics of Complex Traits, Institute of Biomedical and Clinical Science, University of Exeter Medical School, Royal Devon and Exeter Hospital, Exeter, United Kingdom.ORCID 0000-0001-8362-2603
Bjørn Olav ÅsvoldK.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.ORCID 0000-0003-3837-2101
Sara J BrownSkin Research Group, School of Medicine, University of Dundee, Dundee, United Kingdom.ORCID 0000-0002-3232-5251
Naveed SattarInstitute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, United Kingdom.
Lavinia PaternosterMedical Research Council (MRC) Integrative Epidemiology Unit, University of Bristol, Bristol, United Kingdom.ORCID 0000-0003-2514-0889
Norwegian University of Science and Technology · NOUniversity of Exeter · GBUniversity of Glasgow · GBUniversity of Bristol · GBUniversity of Michigan · USLancaster University · GBUniversity of Dundee · GB

Funding

ZINC GLUCONATE GLYCINE LOZENGES &VITAMIN C EFFECTS ON COMMON COLDM01RR000042 · NCRR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELSTROM, REBECCA L · 1985 to 2007
$40.8M
Linkage analysis of familial psoriasis(Supplement)R01AR042742 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD · 1994 to 2021
$10.1M
Genetic and Genomic Dissection of Psoriatic ArthritisR01AR063611 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD, GLADMAN, DAFNA D · 2012 to 2023
$6.2M
Functional Genomics of PsoriasisR01AR065183 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELDER, JAMES TILFORD · 2013 to 2016
$1.7M
British Heart Foundation PG/17/21/32844British Heart Foundation RE/13/5/30177Medical Research Council MC_PC_17228Medical Research Council MC_QA137853Medical Research Council MC_UU_00011/1Medical Research Council MC_UU_00011/4Medical Research Council MR/M005070/1Medical Research Council MR/T002239/1NCRR NIH HHS M01 RR000042NIAMS NIH HHS R01 AR042742NIAMS NIH HHS R01 AR063611NIAMS NIH HHS R01 AR065183Wellcome TrustWellcome Trust 104150/Z/14/ZWellcome Trust 106865/Z/15/Z
6 · The paper itself

Abstract

backgroundPsoriasis is a common inflammatory skin disease that has been reported to be associated with obesity. We aimed to investigate a possible causal relationship between body mass index (BMI) and psoriasis. METHODS AND

findingsFollowing a review of published epidemiological evidence of the association between obesity and psoriasis, mendelian randomization (MR) was used to test for a causal relationship with BMI. We used a genetic instrument comprising 97 single-nucleotide polymorphisms (SNPs) associated with BMI as a proxy for BMI (expected to be much less confounded than measured BMI). One-sample MR was conducted using individual-level data (396,495 individuals) from the UK Biobank and the Nord-Trøndelag Health Study (HUNT), Norway. Two-sample MR was performed with summary-level data (356,926 individuals) from published BMI and psoriasis genome-wide association studies (GWASs). The one-sample and two-sample MR estimates were meta-analysed using a fixed-effect model. To test for a potential reverse causal effect, MR analysis with genetic instruments comprising variants from recent genome-wide analyses for psoriasis were used to test whether genetic risk for this skin disease has a causal effect on BMI. Published observational data showed an association of higher BMI with psoriasis. A mean difference in BMI of 1.26 kg/m2 (95% CI 1.02-1.51) between psoriasis cases and controls was observed in adults, while a 1.55 kg/m2 mean difference (95% CI 1.13-1.98) was observed in children. The observational association was confirmed in UK Biobank and HUNT data sets. Overall, a 1 kg/m2 increase in BMI was associated with 4% higher odds of psoriasis (meta-analysis odds ratio [OR] = 1.04; 95% CI 1.03-1.04; P = 1.73 × 10(-60)). MR analyses provided evidence that higher BMI causally increases the odds of psoriasis (by 9% per 1 unit increase in BMI; OR = 1.09 (1.06-1.12) per 1 kg/m2; P = 4.67 × 10(-9)). In contrast, MR estimates gave little support to a possible causal effect of psoriasis genetic risk on BMI (0.004 kg/m2 change in BMI per doubling odds of psoriasis (-0.003 to 0.011). Limitations of our study include possible misreporting of psoriasis by patients, as well as potential misdiagnosis by clinicians. In addition, there is also limited ethnic variation in the cohorts studied.

conclusionsOur study, using genetic variants as instrumental variables for BMI, provides evidence that higher BMI leads to a higher risk of psoriasis. This supports the prioritization of therapies and lifestyle interventions aimed at controlling weight for the prevention or treatment of this common skin disease. Mechanistic studies are required to improve understanding of this relationship.

Indexed as

Body Mass IndexAdolescentAdultAgedFemaleGenome-Wide Association StudyHumansMaleMendelian Randomization AnalysisMiddle AgedObesityPolymorphism, Single NucleotidePsoriasisRisk FactorsYoung Adult

Identifiers

PMID30703100
PMCPMC6354959
OpenAlexW2913651502

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.